A mathematical model for appraisal of the impact of GH binding protein on GH receptor binding.

Growth regulation Pub Date : 1994-03-01
Z Hochberg, M B Youdim, T Amit
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Abstract

Discrepancies between GH measurements and growth rate of children have complicated diagnosis in a variety of clinical conditions. The competition of GH-BP with the GH-receptor towards GH-receptor binding can have a role in these discrepancies. A mathematical model was developed for appraising the availability of GH for receptor binding from measurements of serum GH by RIA and serum GH binding protein (BP) by a binding assay. Eighteen patients with high GH-BP (obesity), normal GH-BP (normal control) or low GH-BP (children, anorexia nervosa or cirrhosis of the liver) were the subjects of this study. Sera of patients with high, normal or low GH-BP levels were analyzed for their competition with [125I]hGH binding to rabbit liver membranes. Serum GH was measured by a commercial polyclonal RIA. Serum GH-BP was measured by a binding assay with dextran-coated charcoal separation. Receptor availability for GH was assessed by displacing of [125I]hGH from rabbit liver membranes. The decline in receptor availability for each hGH value, caused by GH-BP competition with the receptor, was calculated by subtraction of the percent displacement in the absence of GH-BP from the percent displacement in the presence of a given GH-BP value. The results were analyzed statistically to give a series of polynomes. These enabled the calculation of an activity factor for serum RIA GH levels, that should predict the receptor availability of each GH level, according to the concomitant GH-BP level.(ABSTRACT TRUNCATED AT 250 WORDS)

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一个评估生长激素结合蛋白对生长激素受体结合影响的数学模型。
生长激素测量值与儿童生长速度之间的差异在各种临床条件下使诊断复杂化。GH-BP与gh受体竞争gh受体结合可能在这些差异中起作用。建立了一个数学模型,通过RIA测定血清GH和结合试验测定血清GH结合蛋白(BP)来评估GH对受体结合的有效性。18例高GH-BP(肥胖)、正常GH-BP(正常对照)或低GH-BP(儿童、神经性厌食症或肝硬化)患者为本研究的对象。分析了高、正常和低GH-BP水平患者的血清与[125I]hGH结合兔肝膜的竞争情况。血清生长激素用商用多克隆RIA测定。用葡聚糖包被炭分离结合法测定血清GH-BP。通过从兔肝膜中置换[125I]生长激素来评估生长激素受体的可用性。每个hGH值的受体可用性下降是由GH-BP与受体的竞争引起的,计算方法是用给定GH-BP值时的排水量百分比减去没有GH-BP值时的排水量百分比。对结果进行统计分析,得到一系列多项式。这使得计算血清RIA GH水平的活性因子成为可能,根据伴随的GH- bp水平,该因子可以预测每个GH水平的受体可用性。(摘要删节250字)
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